US11021373B2 - Ammonia production plant and ammonia production method - Google Patents
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- US11021373B2 US11021373B2 US16/762,605 US201816762605A US11021373B2 US 11021373 B2 US11021373 B2 US 11021373B2 US 201816762605 A US201816762605 A US 201816762605A US 11021373 B2 US11021373 B2 US 11021373B2
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- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 title claims abstract description 329
- 229910021529 ammonia Inorganic materials 0.000 title claims abstract description 164
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 63
- 239000007789 gas Substances 0.000 claims abstract description 285
- 238000003786 synthesis reaction Methods 0.000 claims abstract description 140
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 135
- 238000002485 combustion reaction Methods 0.000 claims abstract description 79
- 239000002994 raw material Substances 0.000 claims abstract description 64
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 53
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 53
- 238000011084 recovery Methods 0.000 claims abstract description 43
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 36
- 239000001301 oxygen Substances 0.000 claims abstract description 36
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 36
- 230000002194 synthesizing effect Effects 0.000 claims abstract description 29
- 239000000567 combustion gas Substances 0.000 claims abstract description 20
- 239000000446 fuel Substances 0.000 claims abstract description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 86
- 238000002407 reforming Methods 0.000 claims description 73
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 46
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 32
- 238000000926 separation method Methods 0.000 claims description 31
- 238000006243 chemical reaction Methods 0.000 claims description 26
- 229910052757 nitrogen Inorganic materials 0.000 claims description 16
- 238000006057 reforming reaction Methods 0.000 claims description 16
- 239000003345 natural gas Substances 0.000 claims description 15
- 239000003245 coal Substances 0.000 claims description 11
- 238000007254 oxidation reaction Methods 0.000 claims description 7
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 99
- 229910002092 carbon dioxide Inorganic materials 0.000 description 92
- 238000000034 method Methods 0.000 description 20
- 239000003054 catalyst Substances 0.000 description 11
- 239000001257 hydrogen Substances 0.000 description 10
- 229910052739 hydrogen Inorganic materials 0.000 description 10
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 239000001569 carbon dioxide Substances 0.000 description 7
- 239000003546 flue gas Substances 0.000 description 6
- 238000002309 gasification Methods 0.000 description 5
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 4
- 229910052707 ruthenium Inorganic materials 0.000 description 4
- 229910002091 carbon monoxide Inorganic materials 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000006477 desulfuration reaction Methods 0.000 description 3
- 230000023556 desulfurization Effects 0.000 description 3
- 238000005086 pumping Methods 0.000 description 3
- 238000005057 refrigeration Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000011144 upstream manufacturing Methods 0.000 description 3
- 239000002918 waste heat Substances 0.000 description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003575 carbonaceous material Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000008016 vaporization Effects 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003034 coal gas Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 238000010248 power generation Methods 0.000 description 1
- 229910001404 rare earth metal oxide Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000000629 steam reforming Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
- C01B3/32—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
- C01B3/34—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
- C01B3/38—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
- C01B3/382—Multi-step processes
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
- C01C1/00—Ammonia; Compounds thereof
- C01C1/02—Preparation, purification or separation of ammonia
- C01C1/04—Preparation of ammonia by synthesis in the gas phase
- C01C1/0405—Preparation of ammonia by synthesis in the gas phase from N2 and H2 in presence of a catalyst
- C01C1/0447—Apparatus other than synthesis reactors
- C01C1/0452—Heat exchangers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
- B01D53/34—Chemical or biological purification of waste gases
- B01D53/46—Removing components of defined structure
- B01D53/62—Carbon oxides
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B3/00—Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
- C01B3/02—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
- C01B3/32—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
- C01B3/34—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
- C01B3/48—Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents followed by reaction of water vapour with carbon monoxide
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01C—AMMONIA; CYANOGEN; COMPOUNDS THEREOF
- C01C1/00—Ammonia; Compounds thereof
- C01C1/02—Preparation, purification or separation of ammonia
- C01C1/04—Preparation of ammonia by synthesis in the gas phase
- C01C1/0405—Preparation of ammonia by synthesis in the gas phase from N2 and H2 in presence of a catalyst
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/02—Processes for making hydrogen or synthesis gas
- C01B2203/0205—Processes for making hydrogen or synthesis gas containing a reforming step
- C01B2203/0211—Processes for making hydrogen or synthesis gas containing a reforming step containing a non-catalytic reforming step
- C01B2203/0222—Processes for making hydrogen or synthesis gas containing a reforming step containing a non-catalytic reforming step containing a non-catalytic carbon dioxide reforming step
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/02—Processes for making hydrogen or synthesis gas
- C01B2203/0205—Processes for making hydrogen or synthesis gas containing a reforming step
- C01B2203/0227—Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step
- C01B2203/0233—Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step the reforming step being a steam reforming step
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- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
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- C01B2203/0244—Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step the reforming step being an autothermal reforming step, e.g. secondary reforming processes
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- C—CHEMISTRY; METALLURGY
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- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/02—Processes for making hydrogen or synthesis gas
- C01B2203/025—Processes for making hydrogen or synthesis gas containing a partial oxidation step
- C01B2203/0261—Processes for making hydrogen or synthesis gas containing a partial oxidation step containing a catalytic partial oxidation step [CPO]
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- C—CHEMISTRY; METALLURGY
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- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/04—Integrated processes for the production of hydrogen or synthesis gas containing a purification step for the hydrogen or the synthesis gas
- C01B2203/0465—Composition of the impurity
- C01B2203/0475—Composition of the impurity the impurity being carbon dioxide
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- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
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- C01B2203/068—Ammonia synthesis
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- C—CHEMISTRY; METALLURGY
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- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
- C01B2203/08—Methods of heating or cooling
- C01B2203/0805—Methods of heating the process for making hydrogen or synthesis gas
- C01B2203/0838—Methods of heating the process for making hydrogen or synthesis gas by heat exchange with exothermic reactions, other than by combustion of fuel
- C01B2203/0844—Methods of heating the process for making hydrogen or synthesis gas by heat exchange with exothermic reactions, other than by combustion of fuel the non-combustive exothermic reaction being another reforming reaction as defined in groups C01B2203/02 - C01B2203/0294
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- C01B2203/00—Integrated processes for the production of hydrogen or synthesis gas
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- C01B2203/14—Details of the flowsheet
- C01B2203/142—At least two reforming, decomposition or partial oxidation steps in series
Definitions
- the present invention relates to an ammonia production plant and an ammonia production method having high energy saving and environmental friendliness.
- Ammonia has been gaining attention as a new energy carrier and its advantages have been proved in recent supply chain assessments. Further, since CO2 is not discharged during the combustion of ammonia, the ammonia is expected as promising fuel.
- ammonia has been produced by a catalytic reaction using, for example, hydrogen generated by a reforming reaction of a carbon-based material such as a natural gas and nitrogen in the air as raw materials.
- An ammonia production plant is a plant that requires large power.
- examples include a compressor of a cryogenic separation device that separates air into oxygen and nitrogen, a raw material gas compressor that pressurizes a raw material gas of ammonia to a reaction pressure, and a refrigeration compressor that generates cold heat for cooling and separating synthesized ammonia.
- power is generated by steam generated by recovering waste heat from the process.
- separate fuel is burned in a heating furnace so as to generate steam using obtained heat and to increase the amount of steam, a gas turbine is used together, or power is supplied from outside. In this way, the required power is supplied.
- Patent Document 1 As a conventional ammonia production plant contrived to save energy, Patent Document 1 (WO 2015/193108) describes a method of producing ammonia and a derivative of ammonia from a natural gas supply raw material. Patent Document 1 proposes that a gas turbine supplies at least a part of power required by a power user consuming a large amount of power such as a gas compressor. Patent Document 1 describes that a part of the natural gas supply raw material is supplied as fuel to the gas turbine and the power generated by the gas turbine is used for at least a part of the power consumed by the power user. Further, Patent Document 1 also describes that at least a part of the exhaust heat of the gas turbine is recovered as low-grade heat of a heat user of the ammonia production plant.
- CO 2 discharged from the ammonia production plant is separated into process CO 2 recovered by a device (for example, also referred to as Acid Gas Removal, AGR) that separates an acidic gas from a process gas using a chemical absorption method or the like and flue gas CO 2 contained in an exhaust gas discharged from a combustion furnaces due to air combustion of reformers and boilers.
- AGR Acid Gas Removal
- the CO 2 partial pressure in the exhaust gas from air combustion (hereinafter, flue gas) is low, large energy of 2.5 to 3.0 GJ/ton-CO 2 is required when recovering CO 2 , and hence the thermal efficiency of the plant is remarkably lowered.
- flue gas the CO 2 partial pressure in the exhaust gas from air combustion
- the upper limit of the recovery rate of CO 2 from the flue gas is about 90%, there is a problem that further recovery is difficult.
- Patent Document 1 WO 2015/193108
- the present inventors studied from the viewpoint of the superiority of increasing the energy saving of the plant and reducing CO 2 emissions, found that the above-described problems could be solved by a first aspect and a second aspect below, and completed the invention.
- a first aspect of an ammonia production plant is an ammonia production plant for producing ammonia from a carbon-based raw material, including: an ammonia synthesis facility which synthesizes ammonia; a synthesis gas generating facility which generates a synthesis gas for synthesizing ammonia from the carbon-based raw material; and a power generating facility which obtains power, in which the synthesis gas generating facility includes an exhaust heat recovery unit which recovers exhaust heat generated when generating the synthesis gas, in which the power generating facility includes a combustion device which burns oxygen and fuel and a gas turbine which is driven by using a combustion gas containing a CO 2 gas obtained by the combustion device as power so as to generate power and is configured to supply the CO 2 gas discharged from the gas turbine as a recycle gas to the combustion device, in which the power obtained by the power generating facility is used as at least power of the ammonia synthesis facility, and in which the exhaust heat recovered by the exhaust heat recovery unit is used to heat the recycle gas.
- a second aspect of the ammonia production plant is an ammonia production plant for producing ammonia from a carbon-based raw material, including: an ammonia synthesis facility which synthesizes ammonia; a synthesis gas generating facility which generates a synthesis gas for synthesizing ammonia from the carbon-based raw material; and a power generating facility which obtains power, in which the synthesis gas generating facility includes an exhaust heat recovery unit which recovers exhaust heat generated when generating the synthesis gas, in which the power generating facility includes a combustion device which burns oxygen and fuel, a water vapor generating device which generates water vapor by exhaust heat of a combustion gas containing a CO 2 gas obtained from the combustion device, and a steam turbine which is driven by using the water vapor generated in the water vapor generating device as power so as to generate power and is configured to supply the CO 2 gas discharged from the water vapor generating device as a recycle gas to the combustion device, in which the power obtained by the power generating facility is used
- FIG. 1 illustrates a schematic view of a first aspect of an ammonia production plant according to the invention.
- FIG. 2 illustrates a schematic view of the first aspect of the ammonia production plant according to the invention.
- FIG. 3 illustrates another schematic view of the first aspect of the ammonia production plant according to the invention.
- FIG. 4 illustrates a schematic view of a second aspect of the ammonia production plant according to the invention.
- FIG. 5 illustrates another schematic view of the second aspect of the ammonia production plant according to the invention.
- FIG. 6 illustrates a schematic view of the second aspect of the ammonia production plant according to the invention.
- a positional relationship between devices and facilities may be expressed as “upstream” or “downstream” based on the flow direction of a fluid such as a gas.
- carbon monoxide may be expressed as CO
- carbon dioxide may be expressed as CO 2
- hydrogen may be expressed as H 2 for convenience of description.
- FIG. 1 illustrates a schematic view of a first aspect of an ammonia production plant according to the embodiment.
- An aspect of an ammonia production plant is an ammonia production plant for producing ammonia from a carbon-based raw material, including an ammonia synthesis facility which synthesizes ammonia, a synthesis gas generating facility which generates a synthesis gas for synthesizing ammonia from the carbon-based raw material, and a power generating facility which obtains power.
- the synthesis gas generating facility is a facility which generates a synthesis gas containing H 2 as a main component from the carbon-based raw material.
- the synthesis gas generating facility includes an exhaust heat recovery unit which recovers exhaust heat when generating a synthesis gas.
- the exhaust heat which is recovered by the exhaust heat recovery unit is used to heat a recycle gas to be described later.
- the synthesis gas may contain CO, CO 2 , or methane generated when generating a synthesis gas in addition to H 2 .
- a natural gas or coal (coal gas obtained by gasifying coal) is used as the carbon-based material.
- These raw materials contain hydrocarbons having 1 or more carbon atoms.
- the synthesis gas generating facility When a natural gas is used as the carbon-based raw material, the synthesis gas generating facility reforms the natural gas so as to generate a synthesis gas.
- the exhaust heat recovery unit recovers exhaust heat after the natural gas reforming reaction.
- the synthesis gas generating facility gasifies the coal so as to generate a synthesis gas.
- the exhaust heat recovery unit recovers exhaust heat after the coal gasifying reaction. In the coal gasifying reaction, oxygen reacts with coal so as to generate a synthesis gas.
- the synthesis gas generating facility of the embodiment is configured to recover a CO 2 gas contained in the synthesis gas.
- the synthesis gas generating facility may include a shift reaction unit which reacts carbon monoxide in the synthesis gas obtained by the reforming reaction with water vapor (shift reaction) to generate hydrogen and carbon dioxide.
- the synthesis gas generating facility may include a CO 2 recovery unit which recovers carbon dioxide obtained by the shift reaction (specifically, see FIG. 2 to be described later).
- Exhaust heat generated after reforming a natural gas is recovered by the exhaust heat recovery unit. Further, since the shift reaction is an exothermic reaction, the generated heat can also be recovered in the exhaust heat recovery unit.
- Hydrogen obtained by separating a CO 2 gas from a gas obtained by the shift reaction is sent to the ammonia synthesis facility by a compressor or the like as a raw material gas for the ammonia synthesis reaction.
- ammonia is synthesized by reacting hydrogen generated by the synthesis gas generating facility with nitrogen supplied from a separation device (see FIG. 2 ) to be described later.
- the power generating facility includes a combustion device which burns oxygen and fuel and a gas turbine which is driven by using a combustion gas containing a CO 2 gas obtained by the combustion device as power so as to generate power and is configured to supply the CO 2 gas discharged from the gas turbine as a recycle gas to the combustion device.
- the power generating facility of the embodiment further includes a booster which supplies the CO 2 gas discharged from the gas turbine as a recycle gas to the combustion device.
- the power obtained by the power generating facility is used as at least the power of the ammonia synthesis facility.
- the ammonia synthesis facility is a facility which requires large power and the power obtained by the power generating facility is used as the power of a raw material gas compressor which raises a pressure of a raw material gas (a mixed gas of nitrogen and hydrogen) of ammonia to a reaction pressure and a refrigeration compressor which generates cold heat for cooling and separating the synthesized ammonia.
- the power obtained by the power generating facility may be used as the power of an air compressor installed in the separation device (cryogenic separation device) illustrated in FIG. 2 .
- the power obtained by the power generating facility may be used in the synthesis gas generating facility or the power generating facility.
- the combustion device is a device which burns oxygen and a natural gas so as to obtain a combustion gas containing CO 2 gas and water vapor by the combustion reaction.
- the combustion device of the embodiment burns high-purity oxygen and a natural gas.
- the CO 2 concentration in the obtained combustion gas becomes higher (the CO 2 partial pressure in the combustion gas becomes higher) as compared with a case in which air is supplied to burn a natural gas. For that reason, the energy required for CO 2 gas recovery can be reduced and the CO 2 gas recovery rate can be increased.
- the gas turbine is driven by using the combustion gas containing a CO 2 gas obtained by the combustion device as power.
- the combustion gas of 15 bar to 300 bar and 800° C. to 1300° C. is supplied to the gas turbine and the combustion gas having been used to generate power is discharged from the gas turbine in a state in which the pressure and the temperature are lowered to about 1 bar to 80 bar and 500° C. to 700° C.
- the booster pressurizes the CO 2 gas discharged from the gas turbine.
- CO 2 pressurized by the booster is sent as a recycle gas to the combustion device. Since the state of CO 2 pressurized by the booster is determined by an operation pressure and an operation temperature, CO 2 at the outlet of the booster is a gas, a liquid, or a gas-liquid mixture.
- CO 2 which is pressurized and sent to the combustion device is heated by the exhaust heat recovered by the exhaust heat recovery unit. By this heating, the thermal efficiency of the combustion device can be further improved and a process capable of producing ammonia with far less energy than the conventional method can be constructed.
- the booster pressurizes the CO 2 gas discharged from the gas turbine and the CO 2 gas recovered by the synthesis gas generating facility. That is, the CO 2 gas which is separated and recovered from the synthesis gas generating facility can be combined in the booster and can be sent as a recycle gas to the combustion device.
- the booster can be shared in order to pressurize the CO 2 gas separated and recovered from the synthesis gas generating facility, there is no need to particularly provide a boosting facility in the synthesis gas generating facility and hence the facility cost can be suppressed.
- the synthesis gas generating facility includes a CO 2 recovery unit such as a device for separating an acidic gas by a chemical absorption method using a solvent such as an amine and a separation device for a pressure swing adsorption (PSA) method and a cryogenic separation method (specifically, see FIG. 2 described later) and can separate and recover CO 2 .
- a CO 2 recovery unit such as a device for separating an acidic gas by a chemical absorption method using a solvent such as an amine and a separation device for a pressure swing adsorption (PSA) method and a cryogenic separation method (specifically, see FIG. 2 described later) and can separate and recover CO 2 .
- PSA pressure swing adsorption
- CO 2 Water vapor in the exhaust gas of the gas turbine is separated and recovered as water before pressurizing CO 2 (H 2 O discharged from the booster of FIG. 1 ). Due to the material balance in the facility, CO 2 corresponding to the carbon amount of the carbon-based raw material introduced into the combustion device is discharged to the outside of the power generating facility. The discharged CO 2 may be recovered and used through a technique such as Carbon Dioxide Capture and Storage (CCS) or Enhanced Oil Recovery (EOR).
- CCS Carbon Dioxide Capture and Storage
- EOR Enhanced Oil Recovery
- ammonia production facility By using the exhaust heat of the synthesis gas generating facility and the ammonia synthesis facility (hereinafter, sometimes referred to as ammonia production facility) in the power generating facility, it is possible to further improve the efficiency of the power generating facility and to improve energy saving by effectively using the exhaust heat.
- FIG. 2 illustrates a more preferable aspect of the first aspect of FIG. 1 .
- the synthesis gas generating facility includes a CO 2 recovery unit which recovers a CO 2 gas contained in the synthesis gas.
- the ammonia production plant of the embodiment further includes a separation device which separates air into oxygen and nitrogen.
- the separation device is not particularly limited if oxygen and nitrogen can be separated, but the PSA method or the cryogenic separation method can be used without particular limitation.
- a cryogenic separation type separation device is preferable. In cryogenic separation, air is cooled to a level of ⁇ 180° C. and is liquefied and distilled to separate nitrogen and oxygen and the power generated by the power generating facility is used as the power of the compressor that generates cold heat.
- the separated nitrogen is used in the ammonia synthesis facility.
- the synthesis gas generating facility includes a first reforming unit which reforms the carbon-based raw material and a second reforming unit which reforms the carbon-based raw material not reformed by the first reforming unit. Further, the synthesis gas generating facility may include a shift reaction unit which converts CO generated by the reforming reaction in the first reforming unit and the second reforming unit into CO 2 .
- the shift reaction unit is the same as the aspect illustrated in FIG. 1 .
- the first reforming unit is configured to reform the carbon-based raw material by a water vapor reforming reaction.
- the second reforming unit is configured to reform the carbon-based raw material by a partial oxidation reaction.
- the separation device is configured to supply oxygen to the combustion device and the second reforming unit.
- the first reforming unit mainly reforms a hydrocarbon having 2 or more carbon atoms (a component heavier than methane and hereinafter, sometimes referred to as a C2 plus component). Further, the second reforming unit mainly reforms methane.
- the first reforming unit is provided on the upstream of the second reforming unit.
- the carbon-based raw material in which the C2 plus component is reformed is supplied to the second reforming unit and the carbon-based raw material (that is, mainly methane) not reformed by the first reforming unit can be reformed by the second reforming unit. That is, since the heavy components contained in the carbon-based raw material to be reformed in the second reforming unit are reduced, the generation of unburned carbon is suppressed. Accordingly, it is possible to prolong the life of the catalyst and the device of the second reforming unit operated at a high temperature.
- the water vapor reforming performed in the first reforming unit is an endothermic reaction and the C2 plus component is reformed so that CO and H 2 can be obtained.
- the partial oxidation reaction performed in the second reforming unit is an exothermic reaction and methane is partially oxidized.
- heat is supplied to the water vapor reforming reaction corresponding to an endothermic reaction so that CO and H 2 corresponding to the synthesis gas can be obtained.
- a mixed gas of CO, CO 2 , H 2 , and unreacted methane can be obtained from the second reforming unit.
- the exhaust heat discharged from the second reforming unit is recovered by the exhaust heat recovery unit and a part of the exhaust heat is used for the heating of the first reforming unit and for heating the recycle gas sent to the combustion device.
- High-temperature exhaust heat of 800° C. to 1100° C. is generated at the outlet of the second reforming unit. Conventionally, this heat is used to generate steam of 300° C. to 400° C. and the high-temperature exhaust heat is not efficiently used.
- the high-temperature exhaust heat is used to heat the recycle gas sent to the combustion device and is used for the heating of the first reforming unit. Accordingly, it is possible to further improve the thermal efficiency.
- an auto thermal reformer may be used and the plant can be enlarged.
- self-heating is performed by reaction heat generated by a partial oxidation reaction with oxygen, an external heat supply is not required, and an adiabatic reactor is used. Further, steam reforming also proceeds at the same time by this self-heating.
- the exhaust heat recovery unit includes a high-temperature heat exchanger which recovers high-temperature exhaust heat having a predetermined temperature and a low-temperature heat exchanger which recovers low-temperature exhaust heat having a temperature lower than that of the high-temperature exhaust heat.
- the high-temperature heat exchanger recovers the high-temperature exhaust heat generated in the second reforming unit and the low-temperature heat exchanger recovers the low-temperature exhaust heat generated in the shift reaction unit.
- the high-temperature heat exchanger recovers heat of 500° C. to 1100° C. and the low-temperature heat exchanger recovers heat which is generated by the shift reaction and is lower than the high-temperature exhaust heat.
- the exhaust heat recovered by the exhaust heat recovery unit particularly, apart of the high-temperature exhaust heat is used to heat the recycle gas pressurized by the booster.
- the high-temperature exhaust heat is used to heat the recycle gas
- the heat can be efficiently used and the high-temperature CO 2 gas can be supplied to the combustion device. Accordingly, it is possible to reduce the amount of fuel supplied to the combustion device. For that reason, it is possible to highly efficiently operate the power generating facility as compared with a case in which the recycle gas is not heated by the high-temperature exhaust heat.
- a part of the low-temperature exhaust heat recovered by the low-temperature heat exchanger is used to generate water vapor necessary for at least the water vapor reforming reaction.
- a part of the low-temperature exhaust heat may be used to raise the temperature of the water or may be used as heat for vaporizing water.
- Oxygen obtained by the separation device is supplied to the combustion device of the embodiment.
- the combustion device burns the oxygen and the natural gas. That is, the combustion device of the embodiment burns substantially pure oxygen and the natural gas.
- the oxygen supplied to the combustion device may have high purity.
- a high-concentration oxygen gas having an oxygen concentration of 95% or more may be used for combustion.
- the exhaust heat recovered by the exhaust heat recovery unit is used to heat a CO 2 gas which is a CO 2 gas discharged from the gas turbine and will be supplied to the booster and the recycle gas may be heated by the heated CO 2 gas.
- the power generating device may include a heat exchange unit which is provided between the gas turbine and the booster so as to exchange heat between the CO 2 gas discharged from the gas turbine and the recycle gas (CO 2 gas). Then, the high-temperature exhaust heat recovered by the exhaust heat recovery unit (the high-temperature heat exchanger) may heat the CO 2 gas discharged from the gas turbine and the heat exchange unit may heat the recycle gas by the heated CO 2 gas.
- the recycle gas when the recycle gas is indirectly heated by heating the CO 2 gas discharged from the gas turbine, it is possible to relax the design condition of the high-temperature heat exchanger and to reduce the cost of the high-temperature heat exchanger. That is, when the recycle gas is directly heated at the outlet of the heat exchange unit (when the recycle gas is heated at a position A indicated by the dashed line of FIG. 3 ), designing the high-temperature heat exchanger based on the high-pressure (post-pressurized) recycled gas increases the design pressure of the high-temperature heat exchanger. In contrast, when the CO 2 gas is heated at a position in which a pressure is relatively low, the high-temperature heat exchanger can be designed on the basis of the low-pressure recycle gas and hence the device cost can be reduced.
- FIG. 4 illustrates a schematic view of another aspect of the ammonia production plant according to the invention.
- the same reference numerals will be given to the components common to the first aspect and a description thereof will not be repeated.
- the synthesis gas generating facility includes an exhaust heat recovery unit which recovers exhaust heat generated when generating a synthesis gas
- the power generating facility includes a combustion device which burns oxygen and fuel, a water vapor generating device which generates water vapor by exhaust heat of a combustion gas containing a CO 2 gas obtained from the combustion device, and a steam turbine which is driven by using the water vapor generated in the water vapor generating device as power so as to generate power and is configured to supply the CO 2 gas discharged from the water vapor generating device as a recycle gas to the combustion device
- the power obtained by the power generating facility is used as at least power of the ammonia synthesis facility
- the exhaust heat recovered by the exhaust heat recovery unit is used to generate water vapor in the water vapor generating device.
- the power generating facility includes the gas turbine which is driven by using the combustion gas containing the CO 2 gas obtained by combustion as power and the water vapor generating device generates water vapor by exhaust heat of the gas turbine.
- the aspect of FIG. 4 uses the concept of gas turbine combined cycle power generation.
- the exhaust heat in the exhaust gas discharged from the gas turbine is used as a heat source of the water vapor generating device and water vapor is generated by using the exhaust heat recovered in the exhaust heat recovery unit as a heat source.
- the CO 2 gas discharged from the water vapor generating device and the gas containing water vapor are pressurized by the booster and are supplied as the recycle gas to the combustion device.
- the high-temperature exhaust gas (about 700° C.) discharged from the gas turbine is heated by the heat recovered by the exhaust heat recovery unit and the heated exhaust gas is supplied to, for example, an exhaust heat recovery boiler which is the water vapor generating device.
- the heated exhaust gas is used as a heat source for generating water vapor and the steam turbine is driven by using the generated water vapor.
- the power generating device may not include the gas turbine.
- the power generating device may include a combustion device and a water vapor generating device and may be configured to supply a CO 2 gas discharged from the water vapor generating device as a recycle gas to the combustion device. Also in this configuration, it is possible to provide a highly energy-saving ammonia production plant capable of reducing an emission amount of a CO 2 gas and recovering the CO 2 gas with high efficiency as a whole.
- FIG. 6 illustrates a more preferable aspect of the second aspect illustrated in FIG. 4 .
- the power generating facility includes a pumping device which carries condensed water used for driving the steam turbine to the water vapor generating device along with water supplied from the outside.
- the condensed water becomes water vapor again in the water vapor generating device and is used to drive the steam turbine. In this way, the condensed water circulates between the water vapor generating device and the pumping device.
- the synthesis gas generating facility is configured to recover a CO 2 gas contained in the synthesis gas and the booster is configured to pressurize the CO 2 gas discharged from the gas turbine and the recovered CO 2 gas.
- the synthesis gas generating facility includes the first reforming unit which reforms the carbon-based raw material and the second reforming unit which reforms the carbon-based raw material not reformed by the first reforming unit.
- the second reforming unit is configured to reform the carbon-based raw material by using a partial oxidation reaction and the separation device is configured to supply oxygen to the combustion device and the second reforming unit.
- the first reforming unit and the second reforming unit are the same as those of the aspect of FIG. 2 and an auto thermal reformer may be used in the second reforming unit.
- the exhaust heat recovery unit includes a high-temperature heat exchanger which recovers high-temperature exhaust heat having a predetermined temperature and a low-temperature heat exchanger which recovers low-temperature exhaust heat having a temperature lower than that of the high-temperature exhaust heat.
- the high-temperature heat exchanger is configured to recover the high-temperature exhaust heat generated in the second reforming unit and the low-temperature heat exchanger is configured to recover the low-temperature exhaust heat generated in the shift reaction unit.
- apart of the high-temperature exhaust heat recovered by the high-temperature heat exchanger is used for the heating of the first reforming unit. Further, the high-temperature exhaust heat recovered by the high-temperature heat exchanger and the low-temperature exhaust heat recovered by the low-temperature heat exchanger are used to generate water vapor in the water vapor generating device. Specifically, the high-temperature exhaust heat recovered by the high-temperature heat exchanger is used to generate water vapor by vaporizing water in the water vapor generating device. Meanwhile, the low-temperature exhaust heat recovered by the low-temperature heat exchanger is used to heat condensed water obtained after driving the steam turbine. For example, the low-temperature heat exchanger is provided on the downstream of the pumping device. In this way, when the exhaust heat is used, the heat can be efficiently used.
- the synthesis gas from which carbon dioxide, which is a catalyst poison for ammonia synthesis, has been removed is sent to a nitrogen cleaning device (not illustrated) as necessary and is sent to an ammonia synthesis facility after removing an inert gas component (also referred to as an inert component) by cryogenic separation.
- the synthesis gas from which carbon dioxide has been removed is sent to a methanation device so that a small amount of carbon monoxide and carbon dioxide remaining in the synthesis gas are converted into methane which becomes inactive to the ammonia synthesis catalyst by the methanation reaction and the methane may be sent to the ammonia synthesis facility.
- Hydrogen and nitrogen obtained in the synthesis gas generating facility and the separation device are pressurized to a synthesis pressure (15 bar to 80 bar) for ammonia synthesis by a compressor (not illustrated) and the temperature rises to an ammonia synthesis reaction start temperature (about 400° C. to 500° C.) so that hydrogen and nitrogen are used for an ammonia synthesis reaction.
- the obtained ammonia is separated and recovered as an ammonia product via a known separation facility such as cooling separation using a refrigeration compressor.
- Ammonia synthesis can be performed by a known ammonia synthesis process.
- an ammonia synthesis process for example, a Haber-Bosch method using an iron-based catalyst can be employed.
- a synthesis reaction is performed under a high pressure of 200 bar or more and is also called a high-pressure method.
- a method of synthesizing ammonia under a low pressure condition using a ruthenium catalyst (low pressure method) can also be adopted.
- a catalyst in which a ruthenium catalyst is carried on a carrier can be used.
- a carrier for carrying ruthenium alumina or a rare earth oxide can be used as a carrier for the catalyst.
- an ammonia synthesis method has been proposed in which hydrogen (ion) supplied through a proton exchange membrane is reacted with nitrogen.
- the auto thermal reformer is adopted in the second reforming unit and high-purity oxygen obtained by the separation device is supplied to the combustion device.
- a flue gas is removed and almost all CO 2 gas discharged from the combustion device can be recovered with energy saving.
- an ammonia production method is an ammonia production method of producing ammonia from a carbon-based raw material, including: an ammonia synthesizing step of synthesizing ammonia; a synthesis gas generating step of generating a synthesis gas for synthesizing ammonia from the carbon-based raw material; and a power generating step of obtaining power, in which the synthesis gas generating step includes a step of recovering exhaust heat generated when generating the synthesis gas, in which the power generating step includes a step of burning oxygen and fuel by a combustion device, a step of generating power by a gas turbine driven by using a combustion gas containing a CO 2 gas obtained by the combustion as power, and a step of supplying the CO 2 gas discharged from the gas turbine as a recycle gas to the combustion
- an ammonia production method is an ammonia production method of producing ammonia from a carbon-based raw material, including: an ammonia synthesizing step of synthesizing ammonia; a synthesis gas generating step of generating a synthesis gas for synthesizing ammonia from the carbon-based raw material; and a power generating step of obtaining power, in which the synthesis gas generating step includes a step of recovering exhaust heat generated when generating the synthesis gas, in which the power generating step includes a step of burning oxygen and fuel by a combustion device, a step of generating water vapor by a water vapor generating device using exhaust heat of a combustion gas containing a CO 2 gas obtained by the combustion, a step of generating power by a steam turbine driven by using the water vapor as power, and a step of supplying the CO 2 gas discharged from the water vapor generating device as a recycle gas to the combustion device, in which in at least the ammonia synthesizing step, the power
- ammonia production method includes a step of generating power by the gas turbine driven by using the combustion gas obtained by the combustion device as power and the exhaust heat of the gas turbine may be used to generate water vapor.
- the embodiment since high-purity oxygen and fuel are burned in the combustion device and the highly efficient power generating facility is adopted, a consumption amount of a raw material for synthesizing ammonia is suppressed. Accordingly, it is possible to construct a highly energy-saving ammonia production plant capable of reducing an emission amount of a CO 2 gas and recovering the discharged CO 2 gas with high efficiency. Further, since a process adopting an auto thermal reformer and not discharging a flue gas is constructed, it is possible to eliminate the loss of expensive solvents used in the CO 2 recovery device for recovering CO 2 in a flue gas and the large energy required for CO 2 separation from solvents. As described above, according to the embodiment, it is possible to reduce the energy consumption amount of the plant by as much as 20% even when the separation device separating air into oxygen and nitrogen is used.
- the separation device can be shared in the synthesis gas generating facility and the power generating facility. For that reason, the facility cost can be suppressed. Further, the separation device may supply nitrogen to the ammonia synthesis facility. In this case, the separation device can be shared in three facilities of the synthesis gas generating facility, the power generating facility, and the ammonia synthesis facility.
- the exhaust heat of the synthesis gas generating facility is used in the power generating facility, it is possible to further improve the efficiency of the power generating facility and to improve the energy saving according to the effective usage of the exhaust heat.
- the ammonia plant can be started up without CO 2 emissions using the waste heat of the power generating facility without a conventional start-up combustion device used only for start-up.
- ammonia production plant of the invention is not limited to the above-described embodiment and can be, of course, modified into various forms in the range not departing from the spirit of the invention.
- the water vapor extracted from the steam turbine may be supplied as the water vapor used in a water vapor reforming reaction to the first reforming unit or the second reforming unit. Further, water vapor may be generated when recovering waste heat (heat generated during ammonia synthesis) discharged from the ammonia synthesis facility and the water vapor may be used as water vapor used in the water vapor reforming reaction in the first reforming unit or the second reforming unit.
- the ammonia production plant may include a desulfurization device which removes sulfur contained in the carbon-based raw material.
- the desulfurization device may be provided in a raw material supply line illustrated in FIG. 1 so that the desulferized carbon-based raw material is supplied to the synthesis gas generating facility and the power generating facility.
- the desulfurization device is shared in the synthesis gas generating facility and the power generating facility, it is possible to reduce the cost of treating wastewater from the power generating facility.
- the exhaust heat generated by the synthesis gas generating facility may be used in the power generating facility so as to improve energy saving.
- an outlet gas of an ammonia synthesis reactor provided in the ammonia synthesis facility may be used to generate water vapor using the water vapor generating device or may be used to heat the recycle gas.
- the synthesis gas generating facility when coal is used as the carbon-based raw material, the synthesis gas generating facility includes a gasification furnace for gasifying coal instead of the first reforming unit and the second reforming unit.
- the exhaust heat recovery unit may recover exhaust heat generated when generating a synthesis gas in the gasification furnace.
- the synthesis gas obtained by the gasification furnace is supplied as fuel to the combustion device.
- the synthesis gas obtained by the gasification furnace may be sent to the shift reaction unit after heavy metal is removed therefrom and the synthesis gas obtained by the shift reaction unit may be supplied as fuel to the combustion device.
- oxygen obtained by the separation device may be supplied to the gasification furnace so as to gasify coal.
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Abstract
Description
Claims (15)
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| PCT/JP2018/018384 WO2019215925A1 (en) | 2018-05-11 | 2018-05-11 | Ammonia production plant and method for producing ammonia |
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| US20210053834A1 US20210053834A1 (en) | 2021-02-25 |
| US11021373B2 true US11021373B2 (en) | 2021-06-01 |
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| US (1) | US11021373B2 (en) |
| JP (1) | JP6664033B1 (en) |
| AU (1) | AU2018423019B2 (en) |
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| WO2024220025A1 (en) * | 2023-04-20 | 2024-10-24 | Agency For Science, Technology And Research | Catalytic process using ammonia as hydrogen source for carbon dioxide conversion |
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| US20060228284A1 (en) * | 2005-04-11 | 2006-10-12 | Schmidt Craig A | Integration of gasification and ammonia production |
| JP2008222480A (en) | 2007-03-12 | 2008-09-25 | Ihi Corp | Method for synthesizing ammonia |
| WO2014042042A1 (en) | 2012-09-12 | 2014-03-20 | 三菱重工業株式会社 | Reforming device and reforming method, device for manufacturing chemical products comprising reforming device, and method for manufacturing chemical products |
| JP2014185583A (en) | 2013-03-22 | 2014-10-02 | Central Research Institute Of Electric Power Industry | Nh3 cogeneration type power generation plant |
| WO2015193108A1 (en) | 2014-06-18 | 2015-12-23 | Casale Sa | Process for production of ammonia and derivatives, in particular urea |
| WO2017149718A1 (en) | 2016-03-03 | 2017-09-08 | 日揮株式会社 | Ammonia production method |
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| DE3320228A1 (en) * | 1983-06-03 | 1984-12-06 | Kraftwerk Union AG, 4330 Mülheim | POWER PLANT WITH AN INTEGRATED COAL GASIFICATION PLANT |
| US7909898B2 (en) * | 2006-02-01 | 2011-03-22 | Air Products And Chemicals, Inc. | Method of treating a gaseous mixture comprising hydrogen and carbon dioxide |
| US10106430B2 (en) * | 2013-12-30 | 2018-10-23 | Saudi Arabian Oil Company | Oxycombustion systems and methods with thermally integrated ammonia synthesis |
-
2018
- 2018-05-11 AU AU2018423019A patent/AU2018423019B2/en not_active Ceased
- 2018-05-11 JP JP2019524477A patent/JP6664033B1/en active Active
- 2018-05-11 US US16/762,605 patent/US11021373B2/en active Active
- 2018-05-11 WO PCT/JP2018/018384 patent/WO2019215925A1/en not_active Ceased
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Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060228284A1 (en) * | 2005-04-11 | 2006-10-12 | Schmidt Craig A | Integration of gasification and ammonia production |
| JP2008535768A (en) | 2005-04-11 | 2008-09-04 | イーストマン ケミカル カンパニー | Integrated gasification and ammonia production |
| JP2008222480A (en) | 2007-03-12 | 2008-09-25 | Ihi Corp | Method for synthesizing ammonia |
| WO2014042042A1 (en) | 2012-09-12 | 2014-03-20 | 三菱重工業株式会社 | Reforming device and reforming method, device for manufacturing chemical products comprising reforming device, and method for manufacturing chemical products |
| JP2014185583A (en) | 2013-03-22 | 2014-10-02 | Central Research Institute Of Electric Power Industry | Nh3 cogeneration type power generation plant |
| WO2015193108A1 (en) | 2014-06-18 | 2015-12-23 | Casale Sa | Process for production of ammonia and derivatives, in particular urea |
| WO2017149718A1 (en) | 2016-03-03 | 2017-09-08 | 日揮株式会社 | Ammonia production method |
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| JP6664033B1 (en) | 2020-03-13 |
| SA520420465B1 (en) | 2023-10-29 |
| JPWO2019215925A1 (en) | 2020-05-28 |
| AU2018423019A1 (en) | 2020-11-19 |
| WO2019215925A1 (en) | 2019-11-14 |
| AU2018423019B2 (en) | 2022-07-28 |
| US20210053834A1 (en) | 2021-02-25 |
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